1 |
Formylation of Alcohol with Formic Acid under Solvent-Free and Neutral Conditions Catalyzed by Free I2 or I2 Generated in Situ from Fe(NO3)3·9H2O/NaI
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Chinese Journal of Catalysis
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2 |
Trichloroisocyanuric acid (TCCA) as a mild and efficient catalyst for the trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) under heterogonous conditions
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CATALYSIS COMMUNICATIONS
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3 |
N,N0-Dibromo-N,N0-1,2-ethanediylbis(benzene sulfonamide) as a novel N-bromo reagent catalyzed tetrahydropyranylation/depyranylation of alcohols and phenols under mild conditions
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CATALYSIS COMMUNICATIONS
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4 |
N,N'-Dibromo-N,N'-1,2-ethanediylbis(benzene sulfonamide) as an Efficient Catalyst for Acetylation and Formylation of Alcohols Under Mild Conditions
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PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
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5 |
p-Toluenesulfonyl Chloride (p-TsCl)-Catalyzed Trimethylsilylation of Hydroxyl Groups Using Hexamethyldisilazane and Their Regeneration Under Mild Conditions: The First Example for Catalytic Application of p-Toluenesulfonyl Chloride
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PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
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6 |
N,N-Dibromo-N,N-1,2-ethanediylbis (Benzene Sulfonamide) as a Novel N-Bromo Reagent–Catalyzed Trimethylsilylation of Alcohols and Phenol With
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Phosphorus Sulfur and Silicon
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7 |
1,3-dibromo-5,5-dimethylhydantoin as an efficient and chemoselective agent for the regeneration of carbonyl compounds from semicarbazones and oximes
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Organic Preparations and Procedures International
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8 |
N,N’-Dibromo-N,N’ 1,2-ethanediylbis(benzenesulphonamide) (BNBBS): a Safe, Neutral and Efficient Reagent for the Oxidation of Primary and Secondary Alcohols to Corresponding Carbonyl Compounds under Mild Conditions
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SOUTH AFRICAN JOURNAL OF CHEMISTRY
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9 |
Convenient trimethylsilylation of hydroxy groups with hexamethyldisilazane under solvent-free conditions
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Organic Preparations and Procedures International
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10 |
Novel and Highly Effective Method for the Trimethylsilylation of Alcohols and Phenols with Hexamethyldisilazane (HMDS), Catalyzed by I2 Generated in situ Using Fe(NO3)3 • 9 H2O/NaI under Heterogeneous and Neutral Conditions
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HELVETICA CHIMICA ACTA
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11 |
A Mild Method for the Protection of Aldehydes as Dithioacetals and Dithiolanes Catalyzed by I2 Generated in situ Using Fe(NO3)3.9H2O/NaI Under Heterogeneous Conditions
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Journal of the Chinese Chemical Society
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12 |
A highly efficient and ecofriendly procedure for tetrahydropyranylation of alcohols and phenols in the presence of in-situ generated I2 under heterogeneous and neutral conditions
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MONATSHEFTE FUR CHEMIE
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13 |
Efficient Oxidation of Alcohols to Carbonyl Compounds by N,N-Dichloro-4-methylbenzenesulfonamide under Mild Conditions
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Journal of the Chinese Chemical Society
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14 |
Efficient Trimethylsilylation of Alcohols and Phenols with HMDS in the Presence of a Catalytic Amount of 1,3-Dibromo-5,5-dimethylhydantoin (DBDMH) as a Safe and Cheap Industrial Chemical
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Journal of the Chinese Chemical Society
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15 |
N-Bromosuccinimide (NBS): a Mild and Efficient Catalyst for Tetrahydropyranylation of Alcohols and Phenols under Solvent-Free Conditions
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Journal of the Chinese Chemical Society
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16 |
Microwave-Assisted Chemoselective Regeneration of Carbonyl Compounds from Oximes by Silica Chromate/WET SiO2 under Solvent-Free Conditions
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Phosphorus Sulfur and Silicon
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17 |
Acylation of alcohols catalyzed by using 1,3-dibromo-5,5-dimethylhydentoin or trichloroisocyanuric acid
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CATALYSIS COMMUNICATIONS
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18 |
A novel application of n-bromosaccharin as a chemoselective and efficient oxidative reagent for oxidation of thiols to disulfides under microwave irradiation
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Journal of the Chinese Chemical Society
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19 |
A New Application of N,N'-dibromo-N,N'-1,2-ethanediylbis(p-toluenesulfonamide) as Selective and Efficient Reagent for the Oxidation of Various Thiols to Disulfides
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Phosphorus Sulfur and Silicon
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20 |
A new application of N-bromosaccharin as a selective and efficient oxidative reagent for regeneration of carbonyl compounds from oximes
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Phosphorus Sulfur and Silicon
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21 |
p-Toluenesulfonyl chloride as a new and effective catalyst for acetylation and formylation of hydroxyl compounds under mild conditions
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Chinese Chemical Letters
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